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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588522Generated: October 26, 2026

Nitric Acid → 6-Chloro-3-nitro-imidazo(1,2-b)pyridazine

https://huagongshe.com/reaction/588522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantSodium HydroxideHCID 14798—
ReactantImidazo(1,2-b)pyridazine, 6-chloro-HCID 138828—
SolventSulfuric AcidHCID 1118—
Product6-Chloro-3-nitro-imidazo(1,2-b)pyridazineHCID 1053598191%

Reaction Steps

6-Chloroimidazo[1,2-b]pyridazine (4.95 g, 31.6 mmol) [purchased from Combi-Blocks] was dissolved in 60 mL concentrated sulfuric acid, cooled in an ice bath, and nitric acid (9.9 mL, 158 mmol) was added dropwise while stirring. The reaction was stirred at 0° C. for 30 minutes, then at ambient temperature for 4.5 hours to reach completion. The reaction was poured onto ice, and the resulting aqueous mixture was neutralized with 50% NaOH aqueous solution and then extracted with EtOAc (3×400 mL). The organic layers were combined and washed with water (2×400 mL) and brine (400 mL), dried (Na2SO4), filtered and concentrated to yield the product as a yellowish powder (5.7 g, 91% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227975B2
Source datasetuspto-grants-2016_01
ORD IDord-c951cea0143b4d58a4d3b65caf39e348
Source noteuspto-grants-2016_01